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Laneige UV TOTAL BASE
Laneige UV TOTAL BASE - 43419-861-25 - (Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE)
Drug Information of Laneige UV TOTAL BASE
| Product NDC: | 43419-861 |
| Proprietary Name: | Laneige UV TOTAL BASE |
| Non Proprietary Name: | Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | .07; .084; .02 mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Laneige UV TOTAL BASE
| Product NDC: | 43419-861 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100915 |
Package Information of Laneige UV TOTAL BASE
| Package NDC: | 43419-861-25 |
| Package Description: | 1 TUBE in 1 CARTON (43419-861-25) > 50 mL in 1 TUBE |
NDC Information of Laneige UV TOTAL BASE
| NDC Code | 43419-861-25 |
| Proprietary Name | Laneige UV TOTAL BASE |
| Package Description | 1 TUBE in 1 CARTON (43419-861-25) > 50 mL in 1 TUBE |
| Product NDC | 43419-861 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100915 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | AMOREPACIFIC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .07; .084; .02 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
